Massachusetts General Hospital, Boston, Massachusetts, USA.
Takeda Development Centre Americas, Inc., Lexington, Massachusetts, USA.
Am J Gastroenterol. 2022 Jan 1;117(1):184-188. doi: 10.14309/ajg.0000000000001521.
This post hoc analysis evaluated the effect of prucalopride on abdominal bloating in participants with chronic idiopathic constipation (CIC) who had moderate to very severe bloating at baseline.
Data from 6 phase 3/4 studies of prucalopride in participants with CIC were pooled. Abdominal bloating was assessed weekly using a 5-point scale (0-4).
The proportion of bloating responders (≥1-point improvement in abdominal bloating score at week 12) was higher in participants treated with prucalopride (62.1%) vs placebo (49.6%).
The prucalopride arm had a higher proportion of bloating responders vs placebo in this study population.
本事后分析评估了普芦卡必利对基线时存在中重度腹胀的慢性特发性便秘(CIC)患者的腹胀的影响。
汇总了普芦卡必利治疗 CIC 参与者的 6 项 3/4 期研究的数据。使用 5 分制(0-4)每周评估一次腹胀。
在第 12 周时,腹胀改善≥1 分的腹胀缓解者比例在普芦卡必利治疗组(62.1%)高于安慰剂组(49.6%)。
在该研究人群中,普芦卡必利组的腹胀缓解者比例高于安慰剂组。